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Amelogenesis Imperfecta with Distal Renal Tubular Acidosis: A Novel Syndrome?

Amelogenesis imperfecta (AI) is a heterogeneous group of inherited dental enamel defects. It has rarely been reported in association with multiorgan syndromes and metabolic disorders. The metabolic disorders that have been reported in association with AI include hypocalciuria, impaired urinary conce...

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Autores principales: Misgar, R. A., Hassan, Z., Wani, A. I., Bashir, M. I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434692/
https://www.ncbi.nlm.nih.gov/pubmed/28553046
http://dx.doi.org/10.4103/0971-4065.202826
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author Misgar, R. A.
Hassan, Z.
Wani, A. I.
Bashir, M. I.
author_facet Misgar, R. A.
Hassan, Z.
Wani, A. I.
Bashir, M. I.
author_sort Misgar, R. A.
collection PubMed
description Amelogenesis imperfecta (AI) is a heterogeneous group of inherited dental enamel defects. It has rarely been reported in association with multiorgan syndromes and metabolic disorders. The metabolic disorders that have been reported in association with AI include hypocalciuria, impaired urinary concentrating ability, and Bartter-like syndrome. In literature, only three cases of AI and distal renal tubular acidosis (dRTA) have been described: two cases in adults and a solitary case in the pediatric age group. Here, we report a child with AI presenting with dRTA; to the best of our knowledge, our reported case is the only second such case in pediatric age group. Our case highlights the importance of recognizing the possibility of renal abnormalities in patients with AI as it will affect the long-term prognosis.
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spelling pubmed-54346922017-05-26 Amelogenesis Imperfecta with Distal Renal Tubular Acidosis: A Novel Syndrome? Misgar, R. A. Hassan, Z. Wani, A. I. Bashir, M. I. Indian J Nephrol Case Report Amelogenesis imperfecta (AI) is a heterogeneous group of inherited dental enamel defects. It has rarely been reported in association with multiorgan syndromes and metabolic disorders. The metabolic disorders that have been reported in association with AI include hypocalciuria, impaired urinary concentrating ability, and Bartter-like syndrome. In literature, only three cases of AI and distal renal tubular acidosis (dRTA) have been described: two cases in adults and a solitary case in the pediatric age group. Here, we report a child with AI presenting with dRTA; to the best of our knowledge, our reported case is the only second such case in pediatric age group. Our case highlights the importance of recognizing the possibility of renal abnormalities in patients with AI as it will affect the long-term prognosis. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5434692/ /pubmed/28553046 http://dx.doi.org/10.4103/0971-4065.202826 Text en Copyright: © 2017 Indian Journal of Nephrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Case Report
Misgar, R. A.
Hassan, Z.
Wani, A. I.
Bashir, M. I.
Amelogenesis Imperfecta with Distal Renal Tubular Acidosis: A Novel Syndrome?
title Amelogenesis Imperfecta with Distal Renal Tubular Acidosis: A Novel Syndrome?
title_full Amelogenesis Imperfecta with Distal Renal Tubular Acidosis: A Novel Syndrome?
title_fullStr Amelogenesis Imperfecta with Distal Renal Tubular Acidosis: A Novel Syndrome?
title_full_unstemmed Amelogenesis Imperfecta with Distal Renal Tubular Acidosis: A Novel Syndrome?
title_short Amelogenesis Imperfecta with Distal Renal Tubular Acidosis: A Novel Syndrome?
title_sort amelogenesis imperfecta with distal renal tubular acidosis: a novel syndrome?
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5434692/
https://www.ncbi.nlm.nih.gov/pubmed/28553046
http://dx.doi.org/10.4103/0971-4065.202826
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